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1,4-Naphthalenedione, 2-[2,2-bis(4-methoxyphenyl)ethenyl]-3-chloro- is a complex organic compound with the molecular formula C21H15ClO4. It is a derivative of 1,4-naphthoquinone, featuring a chloro substituent at the 3-position and a 2,2-bis(4-methoxyphenyl)ethenyl group at the 2-position. This molecule is characterized by its conjugated double bonds and aromatic rings, which contribute to its chemical properties. It is likely to be used in the synthesis of various pharmaceuticals, dyes, or other organic compounds due to its unique structure and reactivity. The presence of methoxy groups and a chlorine atom provides opportunities for further functionalization and reaction with other molecules.

93404-12-7

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93404-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93404-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,0 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93404-12:
(7*9)+(6*3)+(5*4)+(4*0)+(3*4)+(2*1)+(1*2)=117
117 % 10 = 7
So 93404-12-7 is a valid CAS Registry Number.

93404-12-7Downstream Products

93404-12-7Relevant academic research and scientific papers

Photoreactions of Halogeno-1,4-naphthoquinones with Electron-rich Alkenes

Maruyama, Kazuhiro,Imahori, Hiroshi

, p. 257 - 265 (2007/10/02)

Photochemical reactions of 2,3-dichloro-1,4-naphthoquinone with 1,1-diarylethylenes or the related electron-rich alkenes have been investigated by steady-state photoreactions, flash photolysis, and kinetic analyses based on the Stern-Volmer experiment and concentration dependence of quantum yields; there is reasonable agreement between them.In acetonitrile a radical ion pair composed of a quinone radical anion and a 1,1-diarylethylene radical cation was observed, while no intermediate was observed in benzene.Dimerization products derived from radical cations were obtained only in the photoreaction of quinone with 1,1-bis(4-methoxyphenyl)ethylene.

Photoinduced Electron-Transfer-Initiated Aromatic Cyclization

Maruyama, Kazuhiro,Otsuki, Tetsuo,Tai, Seiji

, p. 52 - 60 (2007/10/02)

Photochemical reaction of substituted 1,4-naphthoquinones with 1,1-diarylethylenes led primarily to benzanthracene-7,12-dione derivatives.Evidence was obtained that the photoreaction proceeded via a photoinduced electron-transfer process.Extension of t

REACTION MECHANISM OF ONE-POT SYNTHESIS OF POLYCYCLIC QUINONES - DIRECT EVIDENCE OF PHOTO-INDUCED ELECTRON TRANSFER PROCESS

Maruyama, Kazuhiro,Tai, Seiji,Otsuki, Tetsuo

, p. 843 - 844 (2007/10/02)

Photo-induced cyclocondensation of 2,3-disubstituted 1,4-naphthoquinone (substituents; halogen atom or methoxy group) with 1,1-diarylethylene provides us a powerful one-pot synthetic method of polycyclic quinones.Involvement of electron transfer process i

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